Senior​/Medical Director, Oncology

Volastra Therapeutics, Inc. is a clinical-stage oncology biotech company based in New York City, pioneering novel approaches to treating cancer by targeting chromosomal instability (CIN), a unique vulnerability in cancer. Since its founding in 2019, Volastra has grown to support ongoing discovery efforts and a growing clinical organization.

Our lead pipeline programs focus on two distinct inhibitors of KIF
18A, a novel therapeutic target. VLS-1488, internally discovered, entered clinical trials in Q4 2023 for the treatment of advanced cancers. Sovilnesib, in-licensed from Amgen in 2023, re-entered the clinic in Q2 2024. Both assets have been granted Fast-Track Designation by the FDA.

Volastra is backed by top US and European venture firms such as Arch, Polaris, Vida, Droia, Catalio, and B Capital, alongside strategic investment from Eli  addition to venture funding, Volastra has established partnerships with oncology leaders.

Our senior leadership team is highly experienced, supported by a world-class advisory board.

We are headquartered in West Harlem, New York City, within easy reach of Columbia, Cornell, Memorial Sloan Kettering, and surrounding areas. Please visit  for more information.

JOB DESCRIPTION

The role of Senior/Medical Director, Oncology will report to the Vice President of Clinical Development and work collaboratively with the clinical team towards the development and execution of Volastra’s oncology programs. The role will oversee one or more of Volastra’s clinical trials to ensure successful planning, execution and analysis. The ideal candidate works collaboratively and leads by example, is detail-oriented and self-motivated, and has highly relevant experience in oncology clinical development.

Volastra is a fast-paced biotech company of passionate employees, and there is ample opportunity for the ideal candidate to grow and develop with the organization. Individuals will from time to time have the opportunity to gain experience with projects outside their direct scope of work.

Job is based in NYC and requires weekly in office presence, 2-3 days per week

RESPONSIBILITIES

• Work collaboratively with the entire clinical organization to drive the strategy and execution of the overall clinical development plans of the company.
• Support the design of clinical trials and contribute to writing medically important documents such as protocols, regulatory documents, and study reports.
• With support from clinical science and consultant/CRO partners, provide medical oversight of clinical trials, including medical monitoring, review of important safety events, and appropriate communications with investigators.
• Build and maintain strong relationships with clinical study investigators and other external partners.
• Work closely with translational sciences to ensure successful clinical biomarker plans for assigned clinical studies.
• Ensure compliance with SOPs, GCP, safety reporting, and other applicable regulations
• Travel to critical medical conferences (